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  • Methylboronic acid, 97%, Thermo Scientific Chemicals

    L15589.03
    CAS Number: 13061-96-6See All CAS: 13061-96-6 In Stock

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      PRODUCT NAME
      Pack Size
      PRICE
      QUANTITY
       
      CAT NUM: L15589.03
      Methylboronic acid, 97%, Thermo Scientific Chemicals
      Pack Size: 1GR
      PRICE: 
      CAT NUM: L15589.06
      Methylboronic acid, 97%, Thermo Scientific Chemicals
      Pack Size: 5GR
      PRICE: 

      CAS Number
      13061-96-6
      Pack Size
      1GR, 5GR
      Molecular Formula
      C H5 B O2
      Molecular Weight
      59.86
      MFCD
      00002105
      Storage Temp
      RT
      Brand
      Thermo Scientific - Alfa Aesar

      Reagent used for palladium-catalyzed stille and suzuki-miyaura cross-couplings, microwave-heated heterogeneous palladium (pd)-catalytized reactions, ruthenium (ru)-catalyzed silylation reactions, bis(aminotropone) titanium (ti) catalysts for ethylene polymerizations, enantioselective asymmetric bromoaminocyclization and bromoaminocyclization using amino-thiocarbamate catalysts. Reagent used in preparation of common building blocks for pharmaceuticals and agrochemicals, chrysin analogs by suzuki-miyaura coupling reactions, casein kinase i inhibitors, divergent c-h functionalizations directed by sulfonamide pharmacophores in drug discovery.

      This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.


      Applications
      Reagent used for palladium-catalyzed stille and suzuki-miyaura cross-couplings, microwave-heated heterogeneous palladium (pd)-catalytized reactions, ruthenium (ru)-catalyzed silylation reactions, bis(aminotropone) titanium (ti) catalysts for ethylene polymerizations, enantioselective asymmetric bromoaminocyclization and bromoaminocyclization using amino-thiocarbamate catalysts. Reagent used in preparation of common building blocks for pharmaceuticals and agrochemicals, chrysin analogs by suzuki-miyaura coupling reactions, casein kinase i inhibitors, divergent c-h functionalizations directed by sulfonamide pharmacophores in drug discovery.

      Solubility
      Soluble in water.

      Notes
      Hygroscopic.Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, water, moisture.
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